Evidence map›Paper›PMID 23948297›Full record

ArticleCancer cell2013

A kinase-independent function of CDK6 links the cell cycle to tumor angiogenesis.

Karoline Kollmann, Gerwin Heller, Christine Schneckenleithner, Wolfgang Warsch, Ruth Scheicher, Rene G Ott, Markus Schäfer, Sabine Fajmann, Michaela Schlederer, Ana-Iris Schiefer and 14 more

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Cancer cell, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 176 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
176citing papers in PubMed, 1 pooled it
7.8field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

176 citing papers in PubMed, 1 synthesis or guideline pooled it, 302 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Review
  6. Article
  7. AbioRxiv : the preprint server for biology · 2026
    Article
  8. Article
  9. Review
  10. Review
  11. CMGC Kinases in Viral Infection and Human Disease.Pathogens (Basel, Switzerland) · 2026
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article

116 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors at 9 institutions in 3 countries.

Karoline KollmannInstitute of Pharmacology and Toxicology, University of Veterinary Medicine Vienna, 1210 Vienna, Austria.
Gerwin Heller
Christine Schneckenleithner
Wolfgang Warsch
Ruth Scheicher
Rene G Ott
Markus Schäfer
Sabine Fajmann
Michaela Schlederer
Ana-Iris Schiefer
Ursula Reichart
Matthias Mayerhofer
Christoph Hoeller
Sabine Zöchbauer-Müller
Dontscho Kerjaschki
Christoph Bock
Lukas Kenner
Gerald Hoefler
Michael Freissmuth
Anthony R Green
Richard Moriggl
Meinrad Busslinger
Marcos Malumbres
Veronika Sexl
Medical University of Vienna · ATUniversity of Veterinary Medicine Vienna · ATComprehensive Cancer Center Vienna · ATLudwig Boltzmann Institute for Cancer Research · ATAddenbrooke's Hospital · GBCeMM Research Center for Molecular Medicine · ATMedical University of Graz · ATSpanish National Cancer Research Centre · ESVienna Biocenter · AT

Funding

Austrian Science Fund FWF P 24130Austrian Science Fund FWF P 24297Wellcome Trust 079249Wellcome Trust 100140
6 · The paper itself

Abstract

In contrast to its close homolog CDK4, the cell cycle kinase CDK6 is expressed at high levels in lymphoid malignancies. In a model for p185BCR-ABL+ B-acute lymphoid leukemia, we show that CDK6 is part of a transcription complex that induces the expression of the tumor suppressor p16INK4a and the pro-angiogenic factor VEGF-A. This function is independent of CDK6's kinase activity. High CDK6 expression thus suppresses proliferation by upregulating p16INK4a, providing an internal safeguard. However, in the absence of p16INK4a, CDK6 can exert its full tumor-promoting function by enhancing proliferation and stimulating angiogenesis. The finding that CDK6 connects cell-cycle progression to angiogenesis confirms CDK6's central role in hematopoietic malignancies and could underlie the selection pressure to upregulate CDK6 and silence p16INK4a.

Indexed as

AnimalsCell CycleCyclin-Dependent Kinase 6HumansLeukemia, B-CellLymphoma, B-CellMiceMice, Inbred C57BLMice, NudeMice, TransgenicNeoplasmsNeovascularization, PathologicCyclin-Dependent Kinase 6

Identifiers

PMID23948297
PMCPMC3743049
OpenAlexW2152600133

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.